Canonical Allele Identifier: PA658801193
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 502679
ClinVar RCV Id: RCV000597548

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000824.1:p.Ala136Ser
CA394715062
NM_000833.5:c.406G>T